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TELEMETRY WAND MODEL

Page Type
Cleared 510(K)
510(k) Number
K855171
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1986
Days to Decision
27 days

TELEMETRY WAND MODEL

Page Type
Cleared 510(K)
510(k) Number
K855171
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1986
Days to Decision
27 days